63807-86-3

Upstream product

• 97185-30-3 3(4'-hydroxy)phenyl-8,8-dimethyl-6,7-dihydro-4H,8H-benzo(1,2-b:5,4-b')dipyran-4-one 
• 98192-33-7 2'-hydroxy-4-methoxymethoxy-2'',2''-dimethyl-2H-pyrano(4',5':6'',5'')chalcone 
• 98192-34-8 1-(7-Hydroxy-2,2-dimethyl-2H-chromen-6-yl)-3,3-dimethoxy-2-(4-methoxymethoxy-phenyl)-propan-1-one 
• 97185-29-0 3-(4'-Methoxy)phenyl-8,8-dimethyl-6,7-dihydro-4H,8H-benzo<1,2-b; 5,4.b'>dipyran-4-one 
• 19013-03-7 6-acetyl-7-hydroxy-2,2-dimethyl-1H-chromene 
• 31273-58-2 1-(7-hydroxy-2,2-dimethylchroman-6-yl)ethanone 
• 143885-61-4 7-hydroxy-6-(4'-methoxy)cinnamoyl-3,4-dihydro-2,2-dimethyl-2H-benzo(1,2b)pyran 
• 98192-31-5 2'-hydroxy-4-methoxymethoxy-3'',4''-dihydro-2'',2''-dimethyl-2H-pyrano(4',5':6'',5'')chalcone 
• 98192-30-4 1-(7-Hydroxy-2,2-dimethyl-chroman-6-yl)-3,3-dimethoxy-2-(4-methoxy-phenyl)-propan-1-one 
• 98192-32-6 1-(7-Hydroxy-2,2-dimethyl-chroman-6-yl)-3,3-dimethoxy-2-(4-methoxymethoxy-phenyl)-propan-1-one 

Relevant academic research and scientific papers

Synthesis of Erythrinin-A and Related Isoflavones

Erythrinin-A (1) is best synthesized by the condensation of 6-acetyl-7-hydroxy-2,2-dimethylchroman (15) with p-methoxymethoxybenzaldehyde in the presence of alkali followed by oxidative rearrangement of the resulting chalcone (16) with Tl(NO3)3 in MeOH, d

SYNTHESIS OF ERYTHRININ A, A NATURALLY OCCURING PYRANOISOFLAVONE

Erythrinin A (10) has been synthesised by the oxidative rearrangement of dihydropyranochalcone 1 with thallium(III)nitrate (TTN) in trimethyl orthoformate (TMOF) to the dimethyl acetal 2, followed by cyclisation to 3, demethylation to 6 and dehydrogenation.Compound 10 could also be obtained from chalcone 4 on similar rearrangement followed by cyclisation, demethoxymethylation and dehydrogenation.In another route, chalcone 7 was oxidatively rearranged with TTN in TMOF, to 8 which on treatment with HCl yielded 10.

THALLIUM(III) NITRATE MEDIATED SYNTHESIS OF ERYTHRININ-A, DIHYDROPYRANO- AND PYRANOISOFLAVONES

Oxidative rearrangement of dihydropyranochalcones using thallium(III) nitrate-trimethylorthoformate (TTN-TMOF) reagent followed by acid catalysed cyclization yields the corresponding dihydropyranoisoflavones in good yields.Dehydrogenation of these isoflavones gave pyranoisoflavones.Demethylation of isoflavone (7) followed by dehydrogenation gave erythrinin-A (16).